Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AVZ7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.656 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.588 |
CLV_PCSK_PC7_1 | 186 | 192 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.458 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.385 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.577 |
DOC_CDC14_PxL_1 | 117 | 125 | PF14671 | 0.593 |
DOC_CYCLIN_RxL_1 | 281 | 290 | PF00134 | 0.576 |
DOC_MAPK_gen_1 | 261 | 267 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 32 | 40 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 32 | 40 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 7 | 14 | PF00069 | 0.468 |
DOC_PP1_RVXF_1 | 318 | 325 | PF00149 | 0.623 |
DOC_PP1_RVXF_1 | 355 | 361 | PF00149 | 0.453 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.576 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 325 | 330 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 98 | 102 | PF00244 | 0.385 |
LIG_Actin_WH2_2 | 269 | 285 | PF00022 | 0.565 |
LIG_Clathr_ClatBox_1 | 267 | 271 | PF01394 | 0.493 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.529 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.458 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.554 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.497 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.493 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.593 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.467 |
LIG_FXI_DFP_1 | 361 | 365 | PF00024 | 0.580 |
LIG_LIR_Nem_3 | 210 | 215 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.505 |
LIG_PCNA_yPIPBox_3 | 292 | 302 | PF02747 | 0.281 |
LIG_Pex14_2 | 360 | 364 | PF04695 | 0.570 |
LIG_SH2_NCK_1 | 238 | 242 | PF00017 | 0.610 |
LIG_SH2_NCK_1 | 99 | 103 | PF00017 | 0.538 |
LIG_SH2_PTP2 | 342 | 345 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.614 |
LIG_SH3_1 | 25 | 31 | PF00018 | 0.538 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.538 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.531 |
LIG_SUMO_SIM_anti_2 | 153 | 159 | PF11976 | 0.587 |
LIG_SUMO_SIM_par_1 | 139 | 146 | PF11976 | 0.572 |
LIG_SUMO_SIM_par_1 | 68 | 73 | PF11976 | 0.524 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.714 |
LIG_TRAF2_1 | 31 | 34 | PF00917 | 0.593 |
LIG_TYR_ITIM | 333 | 338 | PF00017 | 0.604 |
LIG_UBA3_1 | 26 | 35 | PF00899 | 0.488 |
LIG_UBA3_1 | 267 | 275 | PF00899 | 0.493 |
LIG_WRC_WIRS_1 | 230 | 235 | PF05994 | 0.484 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.390 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.488 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.459 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.488 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.474 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.600 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.410 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.488 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.558 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.564 |
MOD_GlcNHglycan | 365 | 369 | PF01048 | 0.452 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.505 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.484 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.376 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.210 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.190 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.410 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.488 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.577 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.472 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.410 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.488 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.474 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.458 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.481 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.636 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.196 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.488 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.488 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.519 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.456 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.410 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.567 |
MOD_SUMO_rev_2 | 175 | 185 | PF00179 | 0.196 |
MOD_SUMO_rev_2 | 255 | 263 | PF00179 | 0.586 |
TRG_DiLeu_BaEn_1 | 290 | 295 | PF01217 | 0.266 |
TRG_DiLeu_BaEn_3 | 33 | 39 | PF01217 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 22 | 27 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 190 | 194 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J8A6 | Bodo saltans | 27% | 100% |
A0A3Q8ILT9 | Leishmania donovani | 91% | 100% |
A4HCK6 | Leishmania braziliensis | 83% | 100% |
A4I024 | Leishmania infantum | 91% | 100% |
P31521 | Pseudomonas chlororaphis | 26% | 92% |
P94400 | Bacillus subtilis (strain 168) | 26% | 97% |
Q4QBI2 | Leishmania major | 92% | 100% |